RecruitingNot Applicable

Virtual Reality Based Mirror Therapy

Turkey (Türkiye)56 participantsStarted 2024-04-01

Plain-language summary

The aim of this study is to examine the effectiveness of 3D virtual reality assisted mirror therapy based rehabilitation applications compared to classical methods used in stroke rehabilitation.

Who can participate

Age range

40 Years – 80 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Have a ischemic stroke * Stroke duration not less than 2 months and not more than 6 months * Individuals with a score of 2b and 3 according to the Thrombolysis in cerebral infarction (TICI) scale * A score of 2 and above according to the upper extremity motor assessment of the NIH stroke scale * Intact depth perception in the Titmus Stereopsis assessment * A score of 24 and above in the Mini-mental test and * Independent sitting balance Exclusion Criteria: * Additional neurologic diseases * Have a head injury * Have a brain tumor * Prior cranial surgery * Psychological disorder or mental problem * Previous stroke * Aphasia and apraxia * Upper extremity amputation

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Fugl-Meyer Assessment

Timeframe: 8 Weeks

Trial details

NCT IDNCT06152328

SponsorAbant Izzet Baysal University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-05-02

Contact for this trial

Ramazan Kurul, Ph.D

(0374) 254 10 00 ramazankurul2@hotmail.com

View on ClinicalTrials.gov More Stroke trials

Who can participate

Age range

40 Years – 80 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.